| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28937878 | 1.000 | 0.080 | 16 | 75479220 | missense variant | G/T | snv | 1 | |||
| rs370335460 | 1.000 | 0.080 | 16 | 75479677 | missense variant | G/A | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs374493344 | 1.000 | 0.080 | 16 | 75479213 | missense variant | C/A;T | snv | 4.1E-06; 8.3E-06 | 1 | ||
| rs376162109 | 1.000 | 0.080 | 16 | 75479272 | missense variant | G/C;T | snv | 1.6E-05; 3.6E-05 | 1 | ||
| rs377617168 | 1.000 | 0.080 | 16 | 75479615 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs377706989 | 1.000 | 0.080 | 16 | 75479215 | missense variant | C/T | snv | 8.3E-06 | 1.4E-05 | 1 | |
| rs529839563 | 1.000 | 0.080 | 16 | 75479254 | frameshift variant | CGGGGTCGCTGAGCAGCGG/- | delins | 1 | |||
| rs68043642 | 1.000 | 0.080 | 16 | 75479764 | missense variant | A/C | snv | 1 | |||
| rs72547536 | 1.000 | 0.080 | 16 | 75478838 | stop gained | G/A | snv | 1 | |||
| rs72547538 | 1.000 | 0.080 | 16 | 75479009 | missense variant | C/T | snv | 4.1E-06 | 1 | ||
| rs72547539 | 1.000 | 0.080 | 16 | 75479026 | missense variant | T/C | snv | 7.4E-05 | 1.4E-05 | 1 | |
| rs72547540 | 1.000 | 0.080 | 16 | 75479083 | missense variant | T/C;G | snv | 7.0E-06 | 1 | ||
| rs72547542 | 1.000 | 0.080 | 16 | 75479332 | missense variant | C/A;G | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs72547543 | 1.000 | 0.080 | 16 | 75479446 | missense variant | G/A | snv | 1 | |||
| rs72547545 | 1.000 | 0.080 | 16 | 75479509 | missense variant | A/C;G | snv | 2.8E-05 | 1 | ||
| rs72547546 | 1.000 | 0.080 | 16 | 75479539 | missense variant | C/A;G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs72547547 | 1.000 | 0.080 | 16 | 75479633 | missense variant | C/A;G | snv | 4.0E-06 | 1 | ||
| rs72547548 | 1.000 | 0.080 | 16 | 75479647 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs72547549 | 1.000 | 0.080 | 16 | 75479738 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs745571211 | 1.000 | 0.080 | 16 | 75479200 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs750219546 | 1.000 | 0.080 | 16 | 75479216 | missense variant | G/A | snv | 8.3E-06 | 1 | ||
| rs758105699 | 1.000 | 0.080 | 16 | 75479464 | missense variant | T/G | snv | 4.0E-06 | 3.5E-05 | 1 | |
| rs758259312 | 1.000 | 0.080 | 16 | 75478844 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs759870075 | 1.000 | 0.080 | 16 | 75479218 | missense variant | G/C;T | snv | 8.3E-06 | 1 | ||
| rs764372925 | 1.000 | 0.080 | 16 | 75478719 | synonymous variant | G/A;T | snv | 4.0E-06 | 1 |